Biogeochemical, isotope geochemical and microbiological investigation of Lake Svetloe (White Sea basin), a meromictic freshwater was carried out in April 2014, when ice thickness was ∼0.5 m, and the ice-covered water column contained oxygen to 23 m depth. Below, the anoxic water column contained ferrous iron (up to 240 μμM), manganese (60 μM), sulfide (up to 2 μM) and dissolved methane (960 μM). The highest abundance of microbial cells revealed by epifluorescence microscopy was found in the chemocline (redox zone) at 23-24.5 m. Oxygenic photosynthesis exhibited two peaks: the major one (0.43 μmol C L day ) below the ice and the minor one in the chemocline zone, where cyanobacteria related to Synechococcus rubescens were detected. The maximum of anoxygenic photosynthesis (0.69 μmol C L day ) at the oxic/anoxic interface, for which green sulfur bacteria Chlorobium phaeoclathratiforme were probably responsible, exceeded the value for oxygenic photosynthesis. Bacterial sulfate reduction peaked (1.5 μmol S L day ) below the chemocline zone. The rates of methane oxidation were as high as 1.8 μmol CH L day at the oxi/anoxic interface and much lower in the oxic zone. Small phycoerythrin-containing Synechococcus-related cyanobacteria were probably involved in accumulation of metal oxides in the redox zone.
Abstract. In contrast to the large number of studies on humic waters from permafrost-free regions and oligotrophic waters from permafrost-bearing regions, the bio- and photolability of DOM from the humic surface waters of permafrost-bearing regions has not been thoroughly evaluated. Following standardized protocol, we measured biodegradation (at low, intermediate and high temperatures) and photodegradation (at one intermediate temperature) of DOM in surface waters along the hydrological continuum (depression → stream → thermokarst lake → Pechora River) within a frozen peatland in European Russia. In all systems, within the experimental resolution of 5 % to 10 %, there was no bio- or photodegradation of DOM over a 1-month incubation period. It is possible that the main cause of the lack of degradation is the dominance of allochthonous refractory (soil, peat) DOM in all waters studied. However, all surface waters were supersaturated with CO2. Thus, this study suggests that, rather than bio- and photodegradation of DOM in the water column, other factors such as peat pore-water DOM processing and respiration of sediments are the main drivers of elevated pCO2 and CO2 emission in humic boreal waters of frozen peat bogs.
-This work represents a concerted effort aimed at understanding the microbiological and chemical evolution of a small boreal lake during the diurnal cycle of photosynthesis. We studied diurnal variation of y 40 dissolved macro-and trace elements, organic carbon and bacterial population dynamics in the surface and bottom water layer of the shallow Vilno Lake in the White Sea basin. Four-days continuous measurements with 6 h sampling steps both at the surface (0.5 m) and on the bottom (4.0 m depth) during no-bloom periods revealed constant concentrations (within ¡ 20-30%) of all major elements (Na, Mg, Si, K, Ca), organic and inorganic carbon and most trace elements (B, V, Cr, Fe, Cu, Ga, As, Rb, Sr, Y, Zr, Sb, Cs, Ba, all REEs, Hf, Pb, Th, U). At the same time, the concentration of some biologically important trace metals (Mo, Mn, Co, Cd) was subjected to variations partially reflecting the change of bacterioplankton concentration. This work enables two types of element behavior to be distinguished during photosynthesis in the water column -constant concentration and sinusoidal variations -depending on their speciation in solution and their affinity to aquatic microorganisms.
Emission of greenhouse gases (GHGs) from inland waters is recognized as highly important and an understudied part of the terrestrial carbon (C) biogeochemical cycle. These emissions are still poorly quantified in subarctic regions that contain vast amounts of surface C in permafrost peatlands. This is especially true in NE European peatlands, located within sporadic to discontinuous permafrost zones which are highly vulnerable to thaw. Initial measurements of C emissions from lentic waters of the Bolshezemelskaya Tundra (BZT; 200,000 km 2) demonstrated sizable CO 2 and CH 4 concentrations and fluxes to the atmosphere in 98 depressions, thaw ponds, and thermokarst lakes ranging from 0.5 × 10 6 to 5 × 10 6 m 2 in size. CO 2 fluxes decreased by an order of magnitude as waterbody size increased by > 3 orders of magnitude while CH 4 fluxes showed large variability unrelated to lake size. By using a combination of Landsat-8 and GeoEye-1 images, we determined lakes cover 4% of BZT and thus calculated overall C emissions from lentic waters to be 3.8 AE 0.65 Tg C yr −1 (99% C-CO 2 , 1% C-CH 4), which is two times higher than the lateral riverine export. Large lakes dominated GHG emissions whereas small thaw ponds had a minor contribution to overall water surface area and GHG emissions. These data suggest that, if permafrost thaw in NE Europe results in disappearance of large thermokarst lakes and formation of new small thaw ponds and depressions, GHG emissions from lentic waters in this region may decrease.
The colloidal distribution and size fractionation of organic carbon and trace elements were studied in a seasonally stratified, organic-rich boreal lake, Lake Maselga, located in the European subarctic zone (NW Russia, Arkhangelsk region). This study took place over the course of 5 years in winter (glacial) and summer periods and during the spring and autumn overturn. A newly developed in situ dialysis technique (1, 10, and 50 kDa) and traditional frontal filtration and ultrafiltration (20, 10, 5, 0.22, and 0.025 lm) were used to assess element concentrations at different depths. No significant changes in element concentrations occurred during filtration through sub-colloidal pore-size membranes (20-0.22 lm), suggesting a negligible amount of particulate Fe, OC, and associated trace metals. Large colloids (0.025-0.22 lm) were found to be the main carriers of poorly soluble elements (Fe, Al, Ti, Zr, REEs, Th, and U) during the summer and winter stratification. There was also a clear change in the vertical pattern of the percentage of colloidal Al, Ti, V, Cr, Fe, and Ni during different seasons, and the greatest proportion of colloidal forms was observed during the spring and autumn overturn. This pattern is most likely linked to the dominance of soil (allochthonous) organic carbon, which complexes with trace metals during these periods. During the summer seasons, autochthonous production of small exometabolites or photodegradation increases the concentration of the lowmolecular weight fractions (\1 kDa) that dominate the speciation of divalent heavy metals Electronic supplementary material The online version of this article (in surface horizons. The colloidal status of As (30-60%), which was documented in different seasons along the full depth of the water column, is most likely linked to the presence of organic complexes. The overall results of this study suggest that changes in the colloidal speciation of trace elements with depth in different seasons depend on changes in the redox conditions, the input of soil OM, the biodegradation of plankton biomass releasing dissolved organic matter in the bottom horizons, and in upward diffusion from the sediments.
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